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Exercise-induced BDNF promotes PPARδ-dependent reprogramming of lipid metabolism in skeletal muscle during exercise recovery

  • Wing Suen Chan
  • , Chun Fai Ng
  • , Brian Pak Shing Pang
  • , Miaojia Hang
  • , Margaret Chui Ling Tse
  • , Elsie Chit Yu Iu
  • , Xin Ci Ooi
  • , Xiuying Yang
  • , Jason K. Kim
  • , Chi Wai Lee
  • , Chi Bun Chan*
  • *Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

31 Citations (Scopus)

Abstract

Post-exercise recovery is essential to resolve metabolic perturbations and promote long-term cellular remodeling in response to exercise. Here, we report that muscle-generated brain-derived neurotrophic factor (BDNF) elicits post-exercise recovery and metabolic reprogramming in skeletal muscle. BDNF increased the post-exercise expression of the gene encoding PPARδ (peroxisome proliferator–activated receptor δ), a transcription factor that is a master regulator of lipid metabolism. After exercise, mice with muscle-specific Bdnf knockout (MBKO) exhibited impairments in PPARδ-regulated metabolic gene expression, decreased intramuscular lipid content, reduced β-oxidation, and dysregulated mitochondrial dynamics. Moreover, MBKO mice required a longer period to recover from a bout of exercise and did not show increases in exercise-induced endurance capacity. Feeding naïve mice with the bioavailable BDNF mimetic 7,8-dihydroxyflavone resulted in effects that mimicked exercise-induced adaptations, including improved exercise capacity. Together, our findings reveal that BDNF is an essential myokine for exercise-induced metabolic recovery and remodeling in skeletal muscle.

Original languageEnglish
Article numbereadh2783
JournalScience Signaling
Volume17
Issue number828
DOIs
Publication statusPublished - 19 Mar 2024

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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